Majid Mojarrad - Genetic Mutations

Author Information

Majid Mojarrad is currently affiliated with the Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran. His research spans across various aspects of genetics and molecular biology, reflecting his extensive involvement in the field. His work has significant implications in the clinical diagnosis and understanding of various genetic disorders and cancers.

Research Contributions

Majid Mojarrad has made substantial contributions to the field of genetics. In 2022, his research included the development of a novel biosensor for the sensitive and specific clinical diagnosis of SARS-CoV-2, as well as updates on the genetic and molecular biology of gastric cancer among Iranian patients. His work also delved into the challenges of expressing recombinant human tissue factor in Pichia pastoris. In 2021, he reported on PLA2G6 gene mutations and their association with infantile neuroaxonal degeneration, explored the prognostic significance of cancer/testis antigens in glioblastoma, and identified complex chromosomal rearrangements involving chromosomes 1, 11, and 15. Additionally, he has contributed to understanding the genetics of male infertility, fragile X syndrome, and ciliopathies including Joubert and Meckel syndromes, as well as novel candidate genes implicated in severe lethal skeletal dysplasia.

Aliases

Majid Mojarrad is also known by the following aliases: M Mojarrad, M. Mojarrad, and Majid Mojarrad.

Publication and Citation Metrics

Metric Value
H-index 19
Citation Count 1043
Paper Count 128

Publications:

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